A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207251



Internal ID22355676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62345687..62345915hg38UCSC Ensembl
chr2:62572822..62573050hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14290239, nssv14290240
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207251
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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